ENST00000700228.1:c.1479A>C
|
ENSP00000514865.1:p.Glu493Asp
|
|
ENST00000700229.1:c.647A>C
|
|
|
ENST00000700230.1:c.1223A>C
|
ENSP00000514867.1:n.1223A>C
|
|
ENST00000700231.1:c.1608A>C
|
ENSP00000514868.1:p.Glu536Asp
|
|
ENST00000339562.9:c.1683A>C
MANE Select
|
ENSP00000344479.4:p.Glu561Asp
|
|
ENST00000675870.1:c.*194A>C
|
ENSP00000502739.1:n.*194A>C
|
|
ENST00000339562.8:c.1683A>C
|
ENSP00000344479.4:p.Glu561Asp
|
|
ENST00000409108.6:c.1579A>C
|
ENSP00000386993.2:p.Thr527Pro
|
|
ENST00000409572.5:c.1683A>C
|
ENSP00000386747.1:p.Glu561Asp
|
|
ENST00000417764.5:c.*194A>C
|
ENSP00000415632.1:n.*194A>C
|
|
ENST00000417972.5:c.*194A>C
|
ENSP00000394671.1:n.*194A>C
|
|
ENST00000426264.5:c.1494A>C
|
ENSP00000389986.1:p.Glu498Asp
|
|
ENST00000429376.5:c.1390A>C
|
ENSP00000410952.1:p.Thr464Pro
|
|
NM_006186.3:c.1683A>C
|
NP_006177.1:p.Glu561Asp
|
|
XM_005246621.2:c.1716A>C
|
XP_005246678.1:p.Glu572Asp
|
|
XM_005246622.2:c.1494A>C
|
XP_005246679.1:p.Glu498Asp
|
|
XM_005246623.1:c.1494A>C
|
XP_005246680.1:p.Glu498Asp
|
|
XM_006712553.2:c.1641A>C
|
XP_006712616.1:p.Glu547Asp
|
|
XM_011511246.1:c.1612A>C
|
XP_011509548.1:p.Thr538Pro
|
|
NM_173173.2:c.1494A>C
|
NP_775265.1:p.Glu498Asp
|
|
XM_005246621.4:c.1716A>C
|
XP_005246678.1:p.Glu572Asp
|
|
XM_006712553.4:c.1641A>C
|
XP_006712616.1:p.Glu547Asp
|
|
XM_011511246.2:c.1612A>C
|
XP_011509548.1:p.Thr538Pro
|
|
XM_017004219.2:c.1683A>C
|
XP_016859708.1:p.Glu561Asp
|
|
XM_017004220.2:c.1608A>C
|
XP_016859709.1:p.Glu536Asp
|
|
XR_001738751.2:n.1930A>C
|
|
|
XR_001738752.2:n.1752A>C
|
|
|
XR_427087.4:n.1809A>C
|
|
|
NM_006186.4:c.1683A>C
MANE Select
|
NP_006177.1:p.Glu561Asp
|
|
NM_173173.3:c.1494A>C
|
NP_775265.1:p.Glu498Asp
|
|